Aliya Frederick

Title(s)Assistant Clinical Professor, Neurosciences
SchoolVc-health Sciences-schools
Address9500 Gilman Drive #
La Jolla CA 92093
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    Molecular Maladaptations Following Developmental Loss of D1 Receptor Signaling
    NIH F31DA029499Apr 1, 2010 - Mar 31, 2013
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Child Neurology Foundation - Migraine Overview. 2022. Harshika Satyarthi, MD, MPH; Aliya Frederick, MD, PhD. View Publication.
    2. Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes. Hum Mutat. 2022 03; 43(3):305-315. Yang JH, Friederich MW, Ellsworth KA, Frederick A, Foreman E, Malicki D, Dimmock D, Lenberg J, Prasad C, Yu AC, Anthony Rupar C, Hegele RA, Manickam K, Koboldt DC, Crist E, Choi SS, Farhan SMK, Harvey H, Sattar S, Karp N, Wong T, Haas R, Van Hove JLK, Wigby K. PMID: 35026043; PMCID: PMC8863643.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    3. To Be or No B2: A Rare Cause of Stridor and Weakness in a Toddler. Child Neurol Open. 2021 Jan-Dec; 8:2329048X211030723. Frederick AL, Yang JH, Schneider S, Quade A, Guidugli L, Wigby K, Cameron M. PMID: 34395718; PMCID: PMC8361551.
      View in: PubMed   Mentions:
    4. Triacetyluridine treats epileptic encephalopathy from CAD mutations: a case report and review. Ann Clin Transl Neurol. 2021 01; 8(1):284-287. Frederick A, Sherer K, Nguyen L, Ali S, Garg A, Haas R, Sahagian M, Bui J. PMID: 33249780; PMCID: PMC7818142.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    5. Electroencephalographic Findings in Pediatric Patients with Anti-N-Methyl-D-Aspartate Receptor Encephalitis: The San Diego Experience. Journal of Pediatric Epilepsy. 2020. Aliya Frederick , Jennifer H. Yang , Natalie Guido-Estrada , Jose Soria-Lopez , Shifteh Sattar. View Publication.
    6. Evidence against dopamine D1/D2 receptor heteromers. Mol Psychiatry. 2015 Nov; 20(11):1373-85. Frederick AL, Yano H, Trifilieff P, Vishwasrao HD, Biezonski D, Mészáros J, Urizar E, Sibley DR, Kellendonk C, Sonntag KC, Graham DL, Colbran RJ, Stanwood GD, Javitch JA. PMID: 25560761; PMCID: PMC4492915.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansAnimalsCells
    7. Neurobehavioral phenotyping of G(aq) knockout mice reveals impairments in motor functions and spatial working memory without changes in anxiety or behavioral despair. Front Behav Neurosci. 2012; 6:29. Frederick AL, Saborido TP, Stanwood GD. PMID: 22723772; PMCID: PMC3377978.
      View in: PubMed   Mentions: 13  
    8. Drugs, biogenic amine targets and the developing brain. Dev Neurosci. 2009; 31(1-2):7-22. Frederick AL, Stanwood GD. PMID: 19372683; PMCID: PMC2786771.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansAnimals
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